BDBM50592887 CHEMBL5197497

SMILES [H][C@]1(O[C@@](C[C@H](O)[C@H]1NC(C)=O)(OCCCSCCNC(=O)c1ccc(cc1)C(=O)NCCSCCCO[C@@]1(C[C@H](O)[C@@H](NC(C)=O)[C@@]([H])(O1)[C@H](O)[C@H](O)CNC(=O)c1ccc(cc1)-c1ccccc1)C([O-])=O)C([O-])=O)[C@H](O)[C@H](O)CNC(=O)c1ccc(cc1)-c1ccccc1

InChI Key InChIKey=CSMACSVMIFEGCT-UHFFFAOYSA-L

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50592887   

TargetB-cell receptor CD22(Human)
G3-Biotec

Curated by ChEMBL
LigandPNGBDBM50592887(CHEMBL5197497)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of CD22 in human Daudi cells preincubated for 15 mins followed by biotinylated dimeric 2-(78-biotinoylamino-1,4,7,10,13,16-hexaoxa-octadec...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2023
Entry Details
PubMed
TargetB-cell receptor CD22(Human)
G3-Biotec

Curated by ChEMBL
LigandPNGBDBM50592887(CHEMBL5197497)
Affinity DataIC50: 0.410nMAssay Description:Inhibition hFc tagged CD22 incubated for 4 hrs by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2023
Entry Details
PubMed